Production Operator

Organisation:

Natrix Sciences Limited is an EU cGMP-licensed pharmaceutical facility specializing in the development and manufacturing of generic medicines. Operating as a Contract Development and Manufacturing Organisation (CDMO), Natrix focuses on Modified Release Solid Oral Dosage Forms - including powders, granules, and pellets - intended for filling into hard gelatin capsules and tablets.

With a growing reputation for excellence, Natrix has also positioned itself as a strategic partner in innovative research and development projects, particularly in emerging and dynamic industries.

In addition to its core pharmaceutical operations, Natrix Sciences provides specialized services as ZenPharm Limited, a licensed producer of medicinal cannabis. ZenPharm is well-placed to become a local industry leader, and this collaboration offers unique cross-sector experience.

Opportunities for Professional Development:

The Production department at Natrix Sciences offers opportunities for professional growth within a dynamic and ambitious team. Candidates joining the company will become part of a team driven by innovation and excellence. Consequently, we require motivated, committed, and resilient team players who can also work on their own initiative.

Specific Duties and Responsibilities:

The successful candidate will be responsible for:

• To dispense raw materials.

• To perform the processes of various pharmaceutical solid dosage forms and to operate all machinery required for these processes.

• To clean all the equipment/area used in the above processes

• To participate in pharmaceutical production/packaging in the cGMP facility according to the exigencies of Natrix Sciences Ltd.

• To keep the highest quality considerations always in mind during all production / packaging processes whilst striving to achieve the necessary output.

• To report any deviations from SOPs/processes and cGMP guidelines.

• To actively participate in training sessions (receiving and delivering)

• To assist other employees in other departments in fulfilling the common quality goals.

• To follow all applicable safety procedures.

• Ensuring GMP compliance as per local procedures and EudraLex Volume 4 GMP guidelines.

Requirements:

• An ordinary level standard of education.

• Good written and verbal communication skills in both English and Maltese.

• Possession of an EU work visa.

The ideal candidate will be capable of working efficiently and effectively, and be a good team player. The chosen candidate must exhibit strong interpersonal skills and a willingness to learn continuously, be well-educated, be organized, have an eye for detail, and have good communication skills.